Clonidine Transdermal System 0.2mg Recall
Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufactured by: Actavis Lab
Updated March 19, 2026
Clonidine Transdermal System 0.2 mg/day patches supplied by Teva Pharmaceuticals have been recalled because the manufacturer used an unapproved raw material that does not meet required manufacturing standards. This could affect the safety and quality of the medication.
Is the Teva Pharmaceuticals USA, Inc recalled? Yes. This product was recalled by FDA on March 19, 2026. Details below.
What is recalled
Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers (Rx only). Manufactured by Actavis Laboratories UT Inc., Salt Lake City, UT. Distributed by Actavis Pharma, Inc, Parsippany, NJ. NDC 0591-3509-04 (carton) and NDC 0591-3509-54 (pouch).
Am I affected
You are affected if you use or have a prescription for Clonidine Transdermal System 0.2 mg/day patches with NDC 0591-3509-04 or 0591-3509-54. Check your medication bottle or carton for these NDC numbers.
What to do right now
Stop using this patch and contact your pharmacist or prescribing doctor immediately. Do not stop taking clonidine without medical guidance, as your doctor may need to provide an alternative medication or formulation to manage your condition safely.
The hazard
CGMP Deviations: use of an unapproved raw material
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0473-2026
- Classification
- Class II
- Recalled
- March 19, 2026
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